Combined Approach to Lysis Utilizing Eptifibatide and Recombinant Tissue-Type Plasminogen Activator in Acute Ischemic Stroke-Full Dose Regimen Stroke Trial
Author(s) -
Opeolu Adeoye,
Heidi Sucharew,
Jane Khoury,
Achala Vagal,
Pamela Schmit,
Irene Ewing,
Steven R. Levine,
Stacie L Demel,
Bryan Eckerle,
Brian Katz,
Dawn Kleindorfer,
Brian Stettler,
Daniel Woo,
Pooja Khatri,
Joseph P. Broderick,
Arthur Pancioli
Publication year - 2015
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.115.010260
Subject(s) - medicine , eptifibatide , interquartile range , regimen , thrombolysis , stroke (engine) , fibrinolytic agent , tissue plasminogen activator , surgery , myocardial infarction , percutaneous coronary intervention , mechanical engineering , engineering
The Combined Approach to Lysis Utilizing Eptifibatide and Recombinant Tissue-Type Plasminogen Activator (r-tPA; CLEAR) in Acute Ischemic Stroke (AIS) and CLEAR-Enhanced Regimen (CLEAR-ER) trials demonstrated safety of reduced dose r-tPA plus the glycoprotein 2b/3a inhibitor, eptifibatide, in AIS compared with r-tPA alone. The objective of the CLEAR-Full Dose Regimen (CLEAR-FDR) trial was to estimate the rate of symptomatic intracerebral hemorrhage (sICH) in AIS patients treated with the combination of full-dose r-tPA plus eptifibatide.
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